Evidence map›Paper›PMID 40333815›Full record

ArticlePloS one2025

Gene expression-based identification of prognostic markers in lung adenocarcinoma.

Annette Salomonsson, Daniel Ehinger, Mats Jönsson, Johan Botling, Patrick Micke, Hans Brunnström, Johan Staaf, Maria Planck

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Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Annette SalomonssonDepartment of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.
Daniel EhingerDepartment of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.
Mats JönssonDepartment of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.
Johan BotlingDepartment of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Patrick MickeDepartment of Immunology, Genetics, and Pathology, Uppsala University, Uppsala, Sweden.
Hans BrunnströmDepartment of Clinical Sciences Lund, Division of Pathology, Lund University, Lund, Sweden.ORCID 0000-0001-7402-138X
Johan StaafDepartment of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.
Maria PlanckDepartment of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMany studies have aimed at identifying additional prognostic tools to guide treatment choices and patient surveillance in lung cancer by assessing the expression of individual proteins through immunohistochemistry (IHC) or, more recently, through gene expression-based signatures. As a proof-of-concept, we used a multi-cohort, gene expression-based discovery and validation strategy to identify genes with prognostic potential in lung adenocarcinoma. The clinical applicability of this strategy was further assessed by evaluating a selection of the markers by IHC. MATERIALS AND

methodsPublicly available gene expression data sets from six microarray-based studies were divided into four discovery and two validation data sets. First, genes associated with overall survival (OS) in all four discovery data sets were identified. The prognostic potential of each identified gene was then assessed in the two validation data sets, and genes associated with OS in both data sets were considered as potential prognostic markers. Finally, IHC for selected potential prognostic markers was performed in two independent and clinically well-characterized lung cancer cohorts. RESULTS AND

conclusionsThe gene expression-based strategy identified 19 genes with correlation to OS in all six data sets. Out of these genes, we selected Ki67, MCM4 and TYMS for further assessment with IHC. Although an independent prognostic ability of the selected markers could not be confirmed by IHC, this proof-of-concept study demonstrates that by employing a gene expression-based discovery and validation strategy, potential prognostic markers can be identified and further assessed by a technique universally applicable in the clinical practice. The concept of studying potential prognostic markers through gene expression-based strategies, with a subsequent evaluation of the clinical utility, warrants further exploration.

Indexed as

Biomarkers, TumorGene Expression Regulation, NeoplasticLung NeoplasmsAdenocarcinoma of LungAgedFemaleGene Expression ProfilingHumansImmunohistochemistryKi-67 AntigenMaleMiddle AgedPrognosisBiomarkers, TumorKi-67 Antigen

Identifiers

PMID40333815
PMCPMC12057878

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